Atlas FDA

JZE

1 FDA 510(k) clearances · Product code

FDA profile

Official device name
Spoon, Ear
Device class
Class I (low risk)
Regulation
21 CFR 874.4420
Medical specialty
Ear, Nose, Throat
Adverse events (MAUDE)
1998: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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RecordFirmDate
CRUCIOMETER (K884483)Orthopedic Systems, Inc.1989-01-18

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